Aug 2026· Journal of food microbiology· Vol 461, pp.
111987
· 0 citations
Medicine
TL;DR
A combined, metabolite-enhanced biocontrol strategy that positions B. subtilis 507 as a promising candidate for sustainable management of postharvest food diseases such as blue mold in apples is presented.
Abstract
Postharvest blue mold in apples caused by Penicillium expansum poses a great risk to food safety. Here, we report on a phytopathogen targeted enrichment strategy that led to the isolation of an endophytic biocontrol agent (BCA), Bacillus subtilis 507, with strong antagonism against P. expansum. Using a unique dual application approach that combines both live BCA and its crude metabolites (Bac + CM), our result showed an enhanced efficacy. Relative to the control, the disease incidence of blue mold in apples was reduced by 45.95% and lesion diameter was limited to 19.18 mm. Untargeted metabolomics identified bioactive compounds, including 3-phenyllactic acid, pipecolic acid, and spermine, suggesting direct antifungal activity and host based modulation. The mechanistic investigations showed that Bac + CM inhibited spore germination up to 37.3%, and depletion of ergosterol with 97.09% cellular membrane leakage. Fungal hyphal deformation and structural collapse were confirmed by SEM. The BCA rapidly colonized apple fruit wounds and surfaces up to 9.4 log10CFU and reduced natural decay to 5.13% without affecting fruit quality. This study presents a combined, metabolite-enhanced biocontrol strategy that positions B. subtilis 507 as a promising candidate for sustainable management of postharvest food diseases such as blue mold in apples.
Sweetpotato black rot, caused by Ceratocystis fimbriata, is a major postharvest disease that leads to substantial storage losses worldwide. In this study, a salt-tolerant rhizobacterial strain, Bacillus albus SSR3, was isolated from the rhizosphere of sweetpotato grown in saline-alkali soil, with broad-spectrum antagonistic activity against postharvest fungal pathogens. LC-MS/MS analysis revealed diverse bioactive metabolites associated with its antifungal activity. Integrated transcriptomic and metabolomic analyses showed that SSR3 bioactive metabolites extensively reprogrammed fungal metabolism, particularly pathways involved in carbohydrate and amino acid metabolism, antioxidant defense, and energy production. These alterations were accompanied by disruption of cell wall and membrane integrity, excessive reactive oxygen species accumulation, and mitochondrial dysfunction, ultimately inhibiting fungal growth. Here, we also found that SSR3 bioactive metabolites effectively inhibited aflatoxin B1 production by Aspergillus flavus and deoxynivalenol accumulation in Fusarium graminearum. In vivo assays further demonstrated that SSR3 bioactive metabolites significantly reduced sweetpotato black rot severity and effectively limited fungal colonization and mycotoxin contamination in stored agricultural commodities. Collectively, our findings demonstrate that B. albus SSR3 suppresses postharvest fungal pathogens through coordinated metabolic reprogramming, oxidative stress induction, and cellular integrity disruption, highlighting its potential as a sustainable biocontrol agent for postharvest disease management.
Feng-Qin Song, Qing-Ru Geng, Bing-Qian Hu et al.· Journal of food microbiology· 0 citations
Grape white rot, a fungal disease caused by Coniella diplodiella, leads to the decay and abscission of leaves and fruits. This disease is recognized as one of the major fungal diseases affecting the grape industry, significantly impacting the quality and yield of grapes. In this study, a seed-derived Streptomyces strain with high biocontrol activity, designated YTU-S40, was isolated from the seeds of Cnidium monnieri (L.). Molecular phylogenetic identification revealed that this isolate belongs to Streptomyces pseudogriseolus. In vitro plate confrontation experiments demonstrated that YTU-S40 exhibited a robust inhibition rate of 76.2% against C. diplodiella. Furthermore, this strain exhibited relatively broad-spectrum antifungal activity, and genomic analysis predicted that its genome harbors 21 biosynthetic gene clusters responsible for secondary metabolite production. In vivo postharvest grape biocontrol assays verified that YTU-S40 significantly reduced the incidence of grape white rot from 94.4% to 1.9%. Untargeted metabolomic profiling suggested that YTU-S40 may produce bioactive antifungal compounds such as antimycins. Collectively, these findings suggest that YTU-S40 holds considerable promise for development as a biocontrol agent.
Genome mining revealed eight biosynthetic gene clusters associated with antimicrobial secondary metabolites, supporting the genomic characterization of strain BS01 and identifying its biosynthetic potential and identifying its biosynthetic potential.
Van T. Tran, P. D. Tran, Don D. Le et al.· Journal of plant diseases an...· 0 citations
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